{"id":4129234,"url":"https://alion.io/job/atricure-rd-engineer-product-development-medtech","title":"R&D Engineer - Product Development, MedTech","company":{"id":2273800,"name":"Atricure","domain":"atricure.com","url":"https://alion.io/company/atricure","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Greenhouse","truth_index":{"grade":"A","score":95,"open_postings":6,"ghost_share":0,"stale_share":0,"repost_share":0,"time_to_fill_p50_days":62,"computed_at":"2026-11-12T10:38:37Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"junior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Mason, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":1,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"21 CFR Part 820","optional":false},{"name":"Design Controls","optional":false},{"name":"Human Factors Engineering","optional":false},{"name":"ISO 13485","optional":false}],"status":"live","first_seen_at":"2026-11-11T22:52:36Z","employer_posted_date":"2026-11-11","last_verified_at":"2026-11-13T02:37:06Z","board_verified":true,"closed_at":null,"days_open":1,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":1},"description":"AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electrophysiologists and cardiothoracic surgeons around the globe use AtriCure technologies for the treatment of Afib and reduction of Afib related complications. AtriCure’s Isolator® Synergy™ Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib. AtriCure’s AtriClip® Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide. AtriCure’s Hybrid AF™ Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. AtriCure’s cryoICE cryoSPHERE® probe is cleared for temporary ablation of peripheral nerves to block pain, providing pain relief in cardiac and thoracic procedures. For more information, visit AtriCure.com or follow us on Twitter @AtriCure.\nWe foster a culture of inclusion by embracing diverse experiences and individuals where everyone’s authentic self is welcome. We offer supporting programs and resources that provide enriching and equitable opportunities for each person to contribute professionally and personally.\nAbout The Role\nThis position will contribute to the research and development of next-generation medical technologies within AtriCure's product development organization. The engineer will work within a cross-functional team environment and be expected to own designated workstreams from concept through testing and documentation. Responsibilities may include serving as a usability lead, designing and executing laboratory testing, developing prototypes, performing data analysis, supporting design verification activities, and contributing to regulatory submissions. The individual will collaborate closely with mechanical, electrical, software, and clinical stakeholders to advance innovative technologies toward commercialization.\nEssential Function of the Position\nDesign, develop, analyze, and test medical devices using various test equipment, and instruments.\nPerform analytical modeling / analysis of new technologies and design implementations in support of achieving clinical outcomes.\nCollaborate with electrical, embedded software, and systems engineering teams during product development activities.\nSupport integration and testing of hardware, software, and system-level solutions.\nSupport preparation of documentation, testing, and technical evidence required for regulatory submissions.\nBuild prototypes using various rapid prototyping methods to test design concepts.\nUse scientific principles to test performance of medical devices. Record data using appropriate tools and analyze with statistical rigor. Develop conclusions, and present recommendations in written and verbal communications.\nBe knowledgeable of surgical techniques, devices and procedures and be comfortable using them in a preclinical lab setting.\nWork with Key Opinion leaders to collect Voice of Customer data and develop and identify product requirements.\nConduct clinical laboratory activities related to new product development, including animal research studies and procedure development.\nAnalyze, specify, develop, and evaluate the usability of a medical device as it relates to safety, and use results to assess and mitigate risk.\nProvide analysis, testing, and reporting to predict and verify the human body response to designed devices.\nContribute to improvement in methods and processes of the product development organization.\nGenerate and document intellectual property.\nPlan and execute design verification testing activities.\nBuild, evaluate, and troubleshoot prototype and test systems.\nAnalyze experimental and performance data to support product development decisions.\nSupport cryo laboratory testing and product evaluation activities.\nPrepare technical documentation supporting product development and design control activities.\nParticipate in usability engineering activities and design validation efforts.\nSupport FDA submission activities and regulatory documentation as required.\nAdditional Functions of the Role\nRegular and predictable work performance\nAbility to work under fast-paced conditions\nAbility to make decisions and use good judgement\nAbility to prioritize various duties and multitask as required\nAbility to successfully work with others\nAdditional duties as assigned\nBasic Qualifications\nBachelor’s degree required in Engineering or Life Sciences discipline or demonstrated equivalent combination of education, training and experience\n1-5 years of experience in engineering, product development, biomedical engineering, medical devices, or a related technical discipline.\nSolid understanding of:Anatomy, physiology, and biophysics\nIn-vitro and in-vivo lab activities\nMedical device design\nClinical procedure development\nLanguage of medicine\n\nFamiliarity with:Design Controls and experience with FDA QSR 21 CFR Part 820 and ISO 13485\nExternal Standards, Design controls, Quality controls, Manufacturing methods\nFDA design controls, product development processes, and regulated medical device environments preferred.\n\nA track record of:Creative problem solving\nPrioritizing tasks and producing deliverables per schedule expectations\nCompletion of significant and broad tasks with limited direct supervision\nDemonstrated proficiencies of communicating best practices\n\nUnderstanding of development life cycle including needs assessment, drafting product requirements, technology development, detail design & manufacturing systems development, regulatory requirements, and product verification / validation\nProficiency acting in integrated process/product teams, as well as coordinating and communicating customer requirements\nExcellent written and oral communication skills\nExperience and success working in team environment\nExperience with data analysis, problem-solving, and troubleshooting\nExperience with International Usability Standards and the practical application of Usability Engineering\nExperience supporting animal studies, preclinical research, or procedural development activities is helpful but not required.\nAbility to read technical specifications, blueprints, and drawings\nAbility to travel 10%\nPreferred Qualifications\nBS in Biomedical Engineering\nMS in Engineering or Life Sciences discipline\nExcellent demonstrated ability with data analysis, problem-solving, and troubleshooting\nTrack record of managing technical development tasks exhibiting comprehensive planning and thorough communication\nExcellent understanding of industry regulations as it pertains to medical devices\nExcellent understanding of external standards, design controls, quality controls, manufacturing methods\nProven track record of generating and documenting intellectual property\nOther Requirements\nAbility to regularly walk, sit, or stand as needed\nAbility to occasionally bend and push/pull as needed\nAbility to pass pre-employment drug screen and background check\nAtriCure has a variety of benefits available for US based employees and their families. Examples include Medical & Dental beginning day 1 of employment, 401K plus match, 30 days of paid Parental Leave, in addition to maternity leave, for new moms and dads, Volunteer Time off, Pet Insurance, and more. Corporate-based employees also have full access to our on-site fitness center and cafeteria. To see a complete list of our benefits, please visit our careers website: https://www.atricure.com/careers-atricure/benefits.\nAtriCure participates in the federal E-Verify program to confirm the identity of and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here https://www.e-verify.gov AtriCure is an Equal Employment Opportunity/Affirmative Action employer and provides Drug Free Workplaces. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national or ethnic origin, age, protected veteran status, status as an individual with disability, sexual orientation, gender identity or any other characteristic protected by federal, state, or local law(s).\nYou may access our global privacy policy here: https://www.atricure.com/privacy","description_format":"text","description_chars":8282,"description_truncated":false,"requirements":{"experience_years_min":1,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":false},"security_clearance":false,"languages":[]},"benefits":["401k plan","Cafeteria","Parental leave"],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Health Care","Surgical Instruments & Devices","Cardiovascular Devices"],"lifecycle":[{"event":"open","at":"2026-11-12T01:59:53Z"}],"visa":[{"country":"US","licensed_sponsor":true,"adverts_offering_sponsorship_24m":0,"sanctioned_now":false,"evidence":"H-1B filings in 12 months: 10 · green card filings: 2","filings_12m":10,"filings_prev_12m":9,"green_card_filings_12m":2,"median_offered_wage_usd":126667,"route":null,"cap_exempt":false,"checked_at":"2026-11-12T07:36:15+00:00","sources":["US Department of Labor: LCA disclosure data (H-1B, H-1B1, E-3)","US Department of Labor: PERM disclosure data (green cards)"],"filings_for_role_12m":0}],"liveness":{"score":86,"band":"hot","label":"Hiring now","p_open":1,"p_active":0.86,"p_room":1,"age_days":0,"expected_fill_days":62,"reasons":["conf:3","win:early","comp:junior"],"computed_at":"2026-11-12T10:38:37Z"},"pay":null,"html_url":"https://alion.io/job/atricure-rd-engineer-product-development-medtech","json_url":"https://alion.io/job/atricure-rd-engineer-product-development-medtech.json","meta":{"generated_at":"2026-11-13T02:54:40Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","about":"Alion is a live layer of people, companies and AI agents: who they are, whether they are real and active right now, what they do and how to work with them, readable by people and by agents and paid per call.","catalog":"https://alion.io/catalog.json","usage":{"tier":"crawler_verified","counted_by":"address","units_charged":1,"used_today":6167,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-11-14T00:00:00Z"}},"offers":[{"id":"company.slices","title":"One company in depth, by slice","status":"live","price":{"credits":0.1,"usd":0.01,"plus_per_slice":{"credits":0.05,"usd":0.005}},"unit":"per company, plus each slice with data","note":"the employer in depth","call":{"mcp_tool":"get_company","arguments":{"id":2273800},"rest":"https://alion.io/mcp/rest/get_company?id=2273800"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Fatricure-rd-engineer-product-development-medtech"},{"id":"market.stats","title":"A market slice: pay, demand and time to fill","status":"free","price":{"credits":0,"usd":0},"unit":"per slice","note":"pay, demand and time to fill for this role and place","call":{"mcp_tool":"market_stats"},"human":"https://alion.io/catalog?offer=market.stats&for=job%2Fatricure-rd-engineer-product-development-medtech"},{"id":"job.search","title":"Open jobs by role, technology, place, pay and visa","status":"live","price":{"credits":0.1,"usd":0.01},"unit":"per posting in a list","note":"similar open postings","call":{"mcp_tool":"search_jobs"},"human":"https://alion.io/catalog?offer=job.search&for=job%2Fatricure-rd-engineer-product-development-medtech"},{"id":"company.verify","title":"Is this company real and active right now","status":"pilot","price":null,"unit":"per company","request":{"url":"https://alion.io/catalog/request","method":"POST","body":"{\"offer\": \"company.verify\", \"for\": \"job/atricure-rd-engineer-product-development-medtech\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Fatricure-rd-engineer-product-development-medtech"}],"agent":{"mcp":"https://alion.io/mcp/jobs","mcp_open":"https://alion.io/mcp/open","next":[{"tool":"get_job","arguments":{"id":4129234}},{"tool":"search_jobs","arguments":{"company":"atricure.com","detail":"compact"}},{"tool":"match_people","arguments":{"job_id":4129234},"note":"people open to offers who fit this vacancy"}],"note":"The same data through MCP tools: https://alion.io/mcp/open needs no sign-in (compact searches, postings, people); https://alion.io/mcp with an Alion account has everything. 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